Gurecká Radana, Koborová Ivana, Csongová Melinda, Šebek Jozef, Šebeková Katarína
Faculty of Medicine, Institute of Molecular BioMedicine, Comenius University, Sasinkova 4, 811 08, Bratislava, Slovakia.
Faculty of Medicine, Institute of Medical Physics, Biophysics, Informatics and Telemedicine, Comenius University, Bratislava, Slovakia.
Glycoconj J. 2016 Aug;33(4):599-606. doi: 10.1007/s10719-016-9696-9. Epub 2016 Jun 14.
In non-diabetics, low levels of soluble receptor for advanced glycations end products (sRAGE) associate with an increased risk of development of diabetes, cardiovascular afflictions, or death. The majority of studies in non-diabetics report an inverse relationship between measures of obesity, cardiometabolic risk factors and sRAGE and/or endogenous secretory RAGE (esRAGE) levels. To elucidate whether this inconsistency is related to the metabolically healthy obese phenotype, or a different impact of the risk factors in presence and absence of obesity, we analyzed data from 2206 apparently healthy adolescents (51 % girls) aged 15-to-19 years. The association of sRAGE levels with soluble vascular adhesion protein-1/semicarbazide sensitive amine oxidase (sVAP-1/SSAO) was also investigated. Centrally obese, including metabolically healthy, adolescents present significantly lower sRAGE and esRAGE, but not sVAP-1, levels in comparison with their lean counterparts. An increasing number of cardiometabolic risk factors did not associate with significant changes in sRAGE, esRAGE or sVAP-1 levels either in lean or in obese subjects. In multivariate analyses, WHtR, hsCRP, markers of glucose homeostasis, renal function, adiponectin, and sVAP-1 associated significantly with sRAGE and esRAGE. SVAP-1 correlated significantly with glycemia, adiponectin, hsCRP, and sRAGE. Thus, in adolescents, a decline in sRAGE and esRAGE precedes the development of metabolic syndrome. When combined, standard and non-standard cardiometabolic risk factors explain only minor proportion in a variability of sRAGE and esRAGE (8 %-11 %); or sVAP-1 (12 %-20 %). Elucidation of pathogenetic mechanisms underlying early decline in sRAGE and esRAGE levels in obese adolescents and their clinical impact with regard to future cardiometabolic health requires further studies.
在非糖尿病患者中,晚期糖基化终产物可溶性受体(sRAGE)水平较低与患糖尿病、心血管疾病或死亡风险增加相关。大多数针对非糖尿病患者的研究报告称,肥胖、心脏代谢风险因素与sRAGE和/或内源性分泌型RAGE(esRAGE)水平之间呈负相关。为了阐明这种不一致是否与代谢健康的肥胖表型有关,或者在有肥胖和无肥胖情况下风险因素的不同影响,我们分析了2206名15至19岁表面健康的青少年(51%为女孩)的数据。还研究了sRAGE水平与可溶性血管黏附蛋白-1/氨基脲敏感胺氧化酶(sVAP-1/SSAO)的关联。与瘦青少年相比,包括代谢健康的青少年在内的中心性肥胖青少年的sRAGE和esRAGE水平显著降低,但sVAP-1水平未降低。无论是瘦人还是肥胖者,越来越多的心脏代谢风险因素与sRAGE、esRAGE或sVAP-1水平的显著变化均无关联。在多变量分析中,腰高比(WHtR)。hsCRP、血糖稳态标志物、肾功能、脂联素和sVAP-1与sRAGE和esRAGE显著相关。SVAP-1与血糖、脂联素、hsCRP和sRAGE显著相关。因此,在青少年中,sRAGE和esRAGE水平下降先于代谢综合征的发生。标准和非标准心脏代谢风险因素综合起来,在sRAGE和esRAGE(8%-11%)或sVAP-1(12%-20%)的变异性中仅占很小比例。阐明肥胖青少年sRAGE和esRAGE水平早期下降的发病机制及其对未来心脏代谢健康的临床影响需要进一步研究。